Variant #0001056809 (NC_000019.9:g.55677776G>A, NM_178837.4:c.147C>T (DNAAF3))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.55677776G>A
DNA change (hg38) -
Published as DNAAF3(NM_001256714.1):c.147C>T (p.T49=), DNAAF3(NM_001256715.2):c.6C>T (p.(Thr2=))
ISCN -
DB-ID DNAAF3_000052 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00798 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAAF3 NM_001256715.1 -/. - c.6C>T r.(?) p.(Thr2=)
SYT5 NM_003180.2 -/. - c.*7076C>T r.(=) p.(=)
DNAAF3 NM_178837.4 -/. - c.147C>T r.(?) p.(Thr49=)


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